Innate Immune Cells and C-Reactive Protein in Acute First-Episode Psychosis and Schizophrenia: Relationship to Psychopathology and Treatment

Autor: Hans-Gert Bernstein, Peter Falkai, Johann Steiner, Bernhard Bogerts, Thomas Frodl, Paul C. Guest, Henrik Dobrowolny, Sabine Bahn, Brisa Simoes Fernandes, Kolja Schiltz, Gabriela Meyer-Lotz, Katrin Borucki, Roland Jacobs
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Male
drug therapy [Schizophrenia]
pharmacology [Antipsychotic Agents]
Leukocyte Count
0302 clinical medicine
physiopathology [Psychotic Disorders]
neutrophils
drug effects [C-Reactive Protein]
immunology [Psychotic Disorders]
Leukocytes
innate immunity
biology
Positive and Negative Syndrome Scale
Middle Aged
drug therapy [Psychotic Disorders]
immunology [Schizophrenia]
Psychiatry and Mental health
medicine.anatomical_structure
C-Reactive Protein
Schizophrenia
Female
eosinophils
monocytes
Antipsychotic Agents
Adult
Psychosis
drug effects [Immunity
Innate]

03 medical and health sciences
Young Adult
Immune system
monocyte-lymphocyte ratio (MLR)
medicine
Humans
ddc:610
blood [Psychotic Disorders]
Innate immune system
business.industry
neutrophil-lymphocyte ratio (NLR)
Multiple sclerosis
Monocyte
drug effects [Leukocytes]
C-reactive protein
medicine.disease
Immunity
Innate

030227 psychiatry
immunology [Immunity
Innate]

Psychotic Disorders
blood [Schizophrenia]
Immunology
biology.protein
physiopathology [Schizophrenia]
business
030217 neurology & neurosurgery
Regular Articles
Follow-Up Studies
Zdroj: Schizophrenia bulletin 46(2), 363-373 (2019). doi:10.1093/schbul/sbz068
Schizophrenia Bulletin
DOI: 10.1093/schbul/sbz068
Popis: Innate immunity has been linked to initiation of Alzheimer’s disease and multiple sclerosis. Moreover, risk of first-episode psychosis (FEP) and schizophrenia (Sz) is increased after various infections in predisposed individuals. Thus, we hypothesized an analogous role of innate immunity with increased C-reactive protein (CRP) in non-affective psychosis. Differential blood count, CRP, neutrophil and monocyte–macrophage activation markers, cortisol and psychotic symptoms (Positive and Negative Syndrome Scale [PANSS]) were assessed in controls (n = 294) and acutely ill unmedicated FEP (n = 129) and Sz (n = 124) patients at baseline and after 6 weeks treatment. Neutrophils, monocytes, and CRP were increased in patients vs controls at baseline (P < .001), and neutrophil and monocyte counts correlated positively with activation markers. Eosinophils were lower at baseline in FEP (P < .001) and Sz (P = .021) vs controls. Differences in neutrophils (P = .023), eosinophils (P < .001), and CRP (P < .001) were also present when controlling for smoking and cortisol, and partially remitted after antipsychotic treatment. FEP patients with high neutrophils (P = .048) or monocytes (P = .021) had higher PANSS-P scores at baseline but similar disease course. CRP correlated with PANSS-P at baseline (ρ = 0.204, P = .012). Improvement of positive symptoms after treatment correlated with declining neutrophils (ρ = 0.186, P = .015) or CRP (ρ = 0.237, P = .002) and rising eosinophils (ρ = −0.161, P = .036). In FEP, normalization of neutrophils (ρ = −0.231, P = .029) and eosinophils (ρ = 0.209, P = .048) correlated with drug dosage. In conclusion, innate immune system activation correlated with PANSS-P, supporting the immune hypothesis of psychosis. Neutrophil and monocyte counts and CRP levels may be useful markers of disease acuity, severity, and treatment response.
Databáze: OpenAIRE